Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425625생성일: 2026년 10월 26일
2-Hydroxyethyl Methacrylate → 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate
https://huagongshe.com/reaction/1425625
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| 반응물 | (7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoate | HCID 14645478 | — |
| 반응물 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 반응물 | 1-Cyclohexyloxyethyl methacrylate | HCID 22995281 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate | HCID 86643210 | — |
반응 단계
Into a 500 ml-volume three-neck flask, 76.4 g (0.36 mol) of 1-cyclohexyloxyethyl methacrylate, 35.3 g (0.18 mol) of 3,4-epoxycyclohexylmethyl methacrylate (Cyclomer M100, produced by Daicel Chemical Industries, Ltd.), 7.8 g (0.06 mol) of 2-hydroxyethyl methacrylate and 300 ml of methyl isobutyl ketone were charged. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) was added thereto as a radical polymerization initiator, and polymerization was allowed to proceed at 80° C. for 6 hours in a nitrogen stream. The reaction solution was cooled and then poured in a large amount of heptane to precipitate a polymer. The crystal was collected by filtration and dissolved in diethylene glycol dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-5 (1-cyclohexyloxyethyl methacrylate/3,4-epoxycyclohexylmethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08932800B2 |
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| 출처 데이터셋 | uspto-grants-2015_01 |
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| ORD ID | ord-4698e2394c2b4f6990241ab9f73e7f12 |
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| 출처 메모 | uspto-grants-2015_01 |
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